ENST00000356839.10:c.873T>G
MANE Select
|
ENSP00000349297.5:p.Ile291Met
|
|
ENST00000322910.9:c.*828T>G
|
ENSP00000325395.5:n.*828T>G
|
|
ENST00000350303.9:c.807T>G
|
ENSP00000344152.5:p.Ile269Met
|
|
ENST00000356839.9:c.873T>G
|
ENSP00000349297.5:p.Ile291Met
|
|
ENST00000543245.6:c.942T>G
|
ENSP00000438689.2:p.Ile314Met
|
|
ENST00000577191.5:n.1045T>G
|
|
|
ENST00000581378.5:c.591T>G
|
|
|
ENST00000582379.1:n.257T>G
|
|
|
NM_000018.3:c.873T>G
|
NP_000009.1:p.Ile291Met
|
|
NM_001033859.2:c.807T>G
|
NP_001029031.1:p.Ile269Met
|
|
NM_001270447.1:c.942T>G
|
NP_001257376.1:p.Ile314Met
|
|
NM_001270448.1:c.645T>G
|
NP_001257377.1:p.Ile215Met
|
|
XM_006721516.2:c.873T>G
|
XP_006721579.2:p.Ile291Met
|
|
XM_011523829.1:c.873T>G
|
XP_011522131.1:p.Ile291Met
|
|
XM_011523830.1:c.873T>G
|
XP_011522132.1:p.Ile291Met
|
|
XR_934021.1:n.980T>G
|
|
|
XR_934022.1:n.980T>G
|
|
|
XR_934023.1:n.980T>G
|
|
|
XM_006721516.3:c.873T>G
|
XP_006721579.2:p.Ile291Met
|
|
XM_011523829.2:c.873T>G
|
XP_011522131.1:p.Ile291Met
|
|
XM_011523830.2:c.873T>G
|
XP_011522132.1:p.Ile291Met
|
|
XM_024450741.1:c.873T>G
|
XP_024306509.1:p.Ile291Met
|
|
XR_934021.2:n.932T>G
|
|
|
XR_934022.2:n.932T>G
|
|
|
XR_934023.2:n.932T>G
|
|
|
NM_000018.4:c.873T>G
MANE Select
|
NP_000009.1:p.Ile291Met
|
|
NM_001033859.3:c.807T>G
|
NP_001029031.1:p.Ile269Met
|
|
NM_001270447.2:c.942T>G
|
NP_001257376.1:p.Ile314Met
|
|
NM_001270448.2:c.645T>G
|
NP_001257377.1:p.Ile215Met
|
|